autism spectrum disorder Flashcards

1
Q

neuro abnormalities in ASD

A

under connectivity of brain
inflammation of glia
decreased purkinje cells in cerebellum
dysfunctional mirror neurons

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2
Q

ASD is a group

A

of neurodevelopment disorders characterized by repetitive and characteristic patterns of behavior difficulties w/ social comm and interaction

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3
Q

dx under the ASD umbrella

A
  • aspergers
  • childhood disintegrative dx
  • pervasive developmental disorders not otherwise specified
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4
Q

ASD dx criteria

A
  • persistent deficits in comm and social interactions
  • restricted, repetitive patterns or behavior, interest, activities
  • symptoms present in early development, although they may be fully realized when social demands exceed capabilities
  • symptoms cause clinically sig impairment in social, occupational or other important areas of function
  • disturbances are not better explained by intellectual disability or global developmental delay
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5
Q

ASD prevalence

A

1 in 68

boys> girls (4-5x higher)

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6
Q

ASD common signs

A

differences may be noticed during infancy - overly focused on specific objects, poor eye contact, little babbling
development may be typical until 2 or 3 yo
parents commonly have concerns by 1st bday

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7
Q

ASD social impairments

A
  • difficulty w/ socially engaging in convo
  • difficulty understanding the feelings of others and expressing their own
  • may not respond to name
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8
Q

ASD communication

A

fluent to no speech, fluent may be awkward/inappropriate, delayed common
repeating phrases, providing unrelated responses
difficulty processing and using non verbal comm
speak only on limited topics that interest them
flat, robot like, sing song voice

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9
Q

ASD repetitive and characteristic behaviors

A
  • arm flapping, rocking/ spinning
  • fixate on objects like wheels on toys
  • may fixate on topic
  • difficulty w/ changes in routine
  • overstim can lead to outbursts
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10
Q

ASD motor function

A

atypical movement patterns during locomotion, reaching, aining
poor coordination
delayed onset of walking, postural asymm, abnormal tone
motor delay observed in 2-3y

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11
Q

ASD gait characteristics

A

instability
reduced ROM at ankle
increased variability of stride length

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12
Q

early indications for eval of ASD

A
  • no babbling by 1
  • no words by 16 mo or 2 word phrases by 2y
  • no response to name
  • loss of perviously acquired lang
  • poor eye contact
  • no smiling or social responsiveness
  • excessive lining up of objects
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13
Q

late indications for eval of ASD

A
  • difficulty making friends
  • impaired ability to initiate or sustain convo
  • absent/impaired imaginative and social play
  • repetitive language
  • abnormal intense interest
  • preoccupation w/ certain objects
  • inflexible adherence to routine
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14
Q

age that ASD dx can be reliable, valid, stable

A

2y

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15
Q

ASD causes

A

likely both genetic and enviro

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16
Q

ASD genetics

A

36-95% identical
0-31% non identical
higher risk of siblings (2-18%)

17
Q

10% of children w/ ASD also have

A

DS
fragile X
tuberous sclerosis or another genetic or chomrosomal disorder

18
Q

modified checklist for ASD in todlers

A

MCHAT
16-48 mo
parent completed questionnaire

19
Q

pervasive developmental disorder screening test 2

A

PDDSTII
18-48 mo
parent completed questionnaire

20
Q

screening tool for ASD in 2yo

A

STAT
24-36 mo
interactive formation w/ the clinician

21
Q

school communication questionnaire

A

SCQ
>4yo
parent completed questionnaire - ASD

22
Q

PT intervention ASD- exercise and PA

A
  • delayed motor skill develop and impaired motor skill performance
  • prone to sedentary lifestyle
  • research is limited and primarily focuses on changes in behavior and social integration
  • swimming
  • better w/ 1on1
23
Q

PT intervention ASD - sensory processing

A

weighted vests and compression garments

brushing and sensory diets